Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Mod Pathol. 2021 Feb;34(2):300-313. doi: 10.1038/s41379-020-00663-z. Epub 2020 Oct 27.
Sporadic reports of t(3;12)(q26.2;p13) indicate that this abnormality is associated with myeloid neoplasms, myelodysplasia, and a poor prognosis. To better characterize neoplasms with this abnormality, we assessed 20 patients utilizing clinicopathological data, cytogenetic, and targeted next-generation sequencing analysis. We also performed literature review of 58 prior reported cases. Patients included ten men and ten women with median age 55.8 years (range, 27.8-78.8). Diagnoses included 11 acute myeloid leukemia (AML, 5 de novo and 6 secondary), 5 myelodysplastic syndromes (MDS, 3 de novo excess blasts-2 and 2 therapy-related), 2 chronic myeloid leukemia BCR-ABL1-positive blast phase (1 de novo and 1 secondary), 1 primary myelofibrosis (secondary), and 1 mixed-phenotype acute leukemia T/myeloid (MPAL, secondary). Morphologic dysplasia was identified in all AML cases (5/5), MDS cases (4/4), therapy-related cases (3/3), half of myeloproliferative neoplasm cases (1/2), and one MPAL case assessed. The t(3;12) was detected de novo and in subsequent workups in 9 and 11 patients, respectively. Seven patients had t(3;12) only and eight patients had additional chromosome 7 abnormalities. Fluorescence in-situ hybridization detected MECOM (n = 11) and ETV6 (n = 7) rearrangements in all cases assessed. FLT3 internal tandem duplication was identified in five (25%) patients. We identified 13 genetic abnormalities in the de novo group (n = 9), and 25 in the secondary disease group (n = 11). All patients received chemotherapy, with seven allogeneic and two autologous stem cell transplantations. At last follow-up, 14 (70%) patients died with median survival of 6.3 months (range, 0.1-17.3) after detection of t(3;12). In summary, t(3;12)(q26.2;p13) is a rare cytogenetic abnormality in myeloid neoplasms. Myelodysplasia, chromosome 7 abnormalities, and high blast counts are common, and the prognosis is poor. Given the close relationship between the presence of this cytogenetic abnormality and the MDS-related changes, we recommend adding t(3;12)(q26.2;p13) to the list of AML with myelodysplasia-related changes defining abnormalities of the World Health Organization 2017 classification of myeloid neoplasms.
散发性报告显示 t(3;12)(q26.2;p13) 与髓系肿瘤、骨髓增生异常和预后不良有关。为了更好地描述具有这种异常的肿瘤,我们利用临床病理数据、细胞遗传学和靶向下一代测序分析评估了 20 名患者。我们还对 58 例先前报道的病例进行了文献回顾。患者包括 10 名男性和 10 名女性,中位年龄为 55.8 岁(范围为 27.8-78.8)。诊断包括 11 例急性髓系白血病(AML,5 例新发和 6 例继发性)、5 例骨髓增生异常综合征(MDS,3 例新发伴过多原始细胞-2 和 2 例治疗相关)、2 例慢性髓系白血病 BCR-ABL1 阳性急变期(1 例新发和 1 例继发性)、1 例原发性骨髓纤维化(继发性)和 1 例混合表型急性白血病 T/髓系(MPAL,继发性)。所有 AML 病例(5/5)、MDS 病例(4/4)、治疗相关病例(3/3)、一半骨髓增生性肿瘤病例(1/2)和 1 例 MPAL 病例均存在形态学发育不良。t(3;12)在 9 例患者中为新发,在另外 11 例患者中为后续检测发现。7 例患者仅存在 t(3;12),8 例患者存在其他 7 号染色体异常。所有评估的病例均通过荧光原位杂交检测到 MECOM(n=11)和 ETV6(n=7)重排。FLT3 内部串联重复在 5 例(25%)患者中被发现。在新发组(n=9)中我们鉴定了 13 种遗传异常,在继发性疾病组(n=11)中鉴定了 25 种遗传异常。所有患者均接受化疗,其中 7 例接受异基因和 2 例接受自体干细胞移植。在最后一次随访时,14 例(70%)患者在检测到 t(3;12)后死亡,中位生存时间为 6.3 个月(范围为 0.1-17.3)。总之,t(3;12)(q26.2;p13)是髓系肿瘤中罕见的细胞遗传学异常。骨髓增生异常、7 号染色体异常和高原始细胞计数较为常见,预后较差。鉴于这种细胞遗传学异常与 MDS 相关变化之间的密切关系,我们建议将 t(3;12)(q26.2;p13)添加到 2017 年世界卫生组织髓系肿瘤分类中伴有 MDS 相关变化的 AML 列表中,以定义异常。